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verdin

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software/verdin

Variant Primer Design

Machine-generated from the listed sources and not yet reviewed by a human.

record
Category
Software & Systems
Subcategory
unknown
License
GPL-3.0(osi)
Status
dormant
Maturity
deployed
Organization
gear-genomics
Country
unknown
Homepage
unknown
Documentation
unknown
Tags
gear-genomics · genome · pcr · primer-design · variant-calling
Regulatory
unknown
built by · 2

Top contributors by commit count, from the project’s public repository. Avatars are served by their origin, not stored here. To be removed from this list, open an issue.

similar by tags

Computed from shared tags, weighted so a rare tag counts for more than a common one. These are suggestions, not curated relationships.

  • indigogear-genomics

    Indigo: SNV and InDel Discovery in Chromatogram traces obtained from Sanger sequencing of PCR products

  • snp-placergenome · variant-calling

    Take information about snps on short sequence reads and accurately place the snps in a reference genome

  • multiPrime is a mismatch-tolerant minimal primer set design tool for large and diverse sequences (e.g. Virus). Here is a web-based version (test: http://multiPrime.cn)

  • Basecalling, alignment, assembly and deconvolution of Sanger Chromatogram trace files

  • µPCR is a project aiming to bring biohacking to the masses through affordable open source hardware kits and software.

  • DeepSomatic is an analysis pipeline that uses a deep neural network to call somatic variants from tumor-normal and tumor-only sequencing data.

sources
  1. api.github.com/repos/gear-genomics/verdin
    retrieved 2026-08-05 · via github-api

    Machine-imported from GitHub search. Last push 2021-10-11, 3 stars, license reported as GPL-3.0. Category and schematic were assigned by keyword heuristics and are unreviewed.

Not yet verified by a human. Correct this record →

machine-readable

/v1/entries/29.json→ .entries["verdin"]

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